510(k) K962359 ยท MKJ Automated External Defibrillators (Non-Wearable)
LIFEPAK 300
| Applicant | Physio-Control Corp., Redmond WA, US |
| Decision | Substantially Equivalent, Nov 6, 1997 |
| Received | Jun 19, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962359
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.